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EUDAMED MANDATORY USE STARTS IN:
Live Webinar: EUDAMED 2026 and Staying on the EU Market
01 April 2026 | 5:00PM - 6:00PM (CET) | English
EUDAMED will become mandatory on May 28, 2026. Join our free, expert-led webinar to understand exactly what you need to do now to stay compliant and avoid costly delays.
IN THIS WEBINAR, YOU WILL LEARN
✓ How to prepare your organization for EUDAMED mandatory use in May 2026
✓ How to ensure your UDI and device data meet EUDAMED requirements and avoid common issues
✓ How to connect your PLM system with global UDI registries
Register Now
Meet the Experts on EUDAMED Compliance
EUDAMED 2026 becomes mandatory on May 28, affecting every medical device manufacturer placing products on the EU market.
Many companies are already struggling with UDI registration, data quality, and compliance deadlines. In this webinar, our experts share real-world experience from companies navigating EUDAMED today.
You’ll discover where manufacturers typically run into challenges, how to avoid common pitfalls, and practical steps you can take to ensure compliance before the deadline.
With guidance from top MedTech leaders, you’ll leave confident in your ability to meet EUDAMED requirements and keep your devices on the EU market.
Lionel Tussau
MedTech Europe
GS1 Global Healthcare
Jeff Holzman
osapiens
David Wolf
PTC
Jay Crowley
USDM Life Sciences
Kim Guihen
USDM Life Sciences
Stay Ahead of These EUDAMED Challenges
UDI Compliance Issues
Incorrect or missing UDIs can block your products from the EU market.
Data Quality & Consistency
Poor or inconsistent data leads to delays, errors, and regulatory risk.
Integration with Internal Systems
Without proper PLM and ERP connections, manual submissions create costly mistakes.
Deadlines & Market Access Requirementss
Missing the May 28, 2026 deadline can prevent your devices from reaching customers.
Get Ready for EUDAMED 2026
Join our expert-led webinar to understand exactly what you need to do now to stay compliant, avoid delays, and keep your products on the EU market.
Register Now
Free EUDAMED Compliance Guides
EUDAMED Compliance Made Simple – Your Guide to Successful Implementation
Get a practical overview of EUDAMED requirements and learn how to prepare, structure, and submit device data successfully.
Download EUDAMED Guide
Mastering Global UDI Compliance: A practical Guide for Medtech Companies
Understand global UDI frameworks and learn how to structure, validate, and manage product data to meet regulatory requirements across markets.
Download the UDI Compliance Guide
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Your EUDAMED Questions, Answered
Frequently Asked Questions (FAQ)
Resource Center
Further Insights
Blog
Read time: 5 minutes
EUDAMED 2026: Why Late Movers Face Serious Compliance Risk
With the European Commission confirming the EUDAMED 2026 rollout, medical device manufacturers must prepare now to meet upcoming registration deadlines for new and existing devices.
Learn more
Whitepaper
Free Download
Product Information Management (PIM) in the Healthcare Industry
Discover how healthcare companies can meet strict product information requirements with the right processes and technology.
Download whitepaper
Blog
Read time: 6 minutes
EUDAMED 2026: Key Steps for Medical Device Manufacturers
With the European Commission confirming the EUDAMED 2026 rollout, medical device manufacturers must prepare now to meet upcoming registration deadlines for new and existing devices.
Learn more
Case Study
Free Download
How PAJUNK® Streamlined Product Content Management with the osapiens HUB for Medical Devices
Discover how PAJUNK® turned slow, error-prone product data into a fully automated, regulation-ready system.
Learn more
Blog
Read time: 6 minutes
Understanding AusUDID: Australia's Unique Device Identification Database
With AusUDID, Australia is joining the global UDI ecosystem, adding a new regulatory requirement for companies supplying medical and IVD devices to the Australian market.
Learn more
Blog
Read time: 7 minutes
swissdamed Explained: Requirements, Deadlines, and What Medical Device Companies Should Do Now
swissdamed is Switzerland’s national medical device database, and manufacturers, authorized representatives, and importers must register their devices and company data before mandatory device registration begins in July 2026.
Learn more
